|
|
||||||||
The Biological Bulletin, Vol 188, Issue 3 255-266, Copyright © 1995 by Marine Biological Laboratory
CELL BIOLOGY |
J. H. Chen and C. J. Bayne
Department of Zoology, Oregon State University, Oregon 97331-2914
Within minutes of removal from the California mussel, Mytilus californianus, hemocytes become sticky for one another and for foreign surfaces. We sought to understand the cell surface changes responsible for this altered state. Hemocyte aggregation and adhesion assays were used in experiments in which a variety of reagents potentially capable of interfering with aggregation were screened. Caffeine, nor-ethylmaleimide, cytochalasin B, and EDTA were completely or partially inhibitory towards aggregation and adhesion. However, RGD-containing peptides, glycosaminoglycans, protease inhibitors, heparin, or poly-L-lysine were without effect. Low temperature (4{deg}C) slowed hemocyte adhesion and hemocyte cohesion. Based on the findings, it appears that (1) Mytilus hemocyte aggregation, in vitro, is a two-step process that requires metabolic energy and divalent cations (calcium and magnesium), and is temperature-sensitive; and (2) Mytilus hemocyte adhesion and hemocyte aggregation are two associated but different cell behaviors.
This article has been cited by other articles:
![]() |
G. G. Martin, C. T. Oakes, H. R. Tousignant, H. Crabtree, and R. Yamakawa Structure and function of haemocytes in two marine gastropods, Megathura crenulata and Aplysia californica J. Mollus. Stud., November 1, 2007; 73(4): 355 - 365. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Canesi, C. Pruzzo, R. Tarsi, and G. Gallo Surface Interactions between Escherichia coli and Hemocytes of the Mediterranean Mussel Mytilus galloprovincialis Lam. Leading to Efficient Bacterial Clearance Appl. Envir. Microbiol., January 1, 2001; 67(1): 464 - 468. [Abstract] [Full Text] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |